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Clinical trial condition

Genetic Diseases, Inborn

Explore clinical trials studying Genetic Diseases, Inborn. Study availability and eligibility vary by location and protocol.

12,619 public trials 2,162 recruiting studies
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Genetic Diseases, Inborn trial results

Completed

Combination Trial of Tipifarnib and Alpelisib in Adult Recurrent/ Metastatic Head and Neck Squamous Cell Carcinoma (R/M HNSCC)

NCT04997902

Conditions
Carcinoma, Carcinoma, Squamous Cell, Congenital Abnormalities, +21 more
Locations
  • City of Hope Comprehensive Cancer Center Duarte, California, United States
  • Lake Nona DDU (Florida Cancer Specialists) Orlando, Florida, United States
  • University of Maryland School of Medicine (Marlene and Stewart Greenebaum Comprehensive Cancer Center) Baltimore, Maryland, United States
  • Johns Hopkins University School of Medicine (Sidney Kimmel Comprehensive Cancer Center) Baltimore, Maryland, United States
View Trial Details
Completed

An Open-label Extension Trial to Evaluate the Long-term Safety of KVD900 (Sebetralstat) for On-Demand Treatment of Angioedema Attacks in Adolescent and Adult Patients With Hereditary Angioedema (HAE)

NCT05505916

Conditions
Angioedema, Angioedemas, Hereditary, Cardiovascular Diseases, +14 more
Locations
  • KalVista Investigative Site Scottsdale, Arizona, United States
  • KalVista Investigative Site Little Rock, Arkansas, United States
  • KalVista Investigative Site San Diego, California, United States
  • KalVista Investigative Site San Diego, California, United States
View all 71 locations
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Completed

Colonoscopy Check-up in People With Lynch Syndrome

NCT06126120

Conditions
Colonic Diseases, Colorectal Neoplasms, Colorectal Neoplasms, Hereditary Nonpolyposis, +15 more
Locations
  • Cancer Screening and Prevention Research Group (CSPRG), Department of Surgery and Cancer, Queen Elizabeth The Queen Mother (QEQM) Building, St Mary's Hospital, Imperial College London London, United Kingdom
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Completed

Dance and Huntington Disease

NCT01842919

Conditions
Basal Ganglia Diseases, Brain Diseases, Central Nervous System Diseases, +13 more
Locations
  • Institut du cerveau et de la moelle épinière (ICM), CHU Pitié Salpêtrière Paris, France
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Completed

Study of ARO-APOC3 (Plozasiran) in Adults With Familial Chylomicronemia Syndrome (FCS)

NCT05089084

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyslipidemias, Familial Chylomicronemia, +9 more
Locations
  • Clinical Site 1 Boca Raton, Florida, United States
  • Clinical Site 2 Suwanee, Georgia, United States
  • Clinical Site 3 Indianapolis, Indiana, United States
  • Clinical Site 4 Elkridge, Maryland, United States
View all 58 locations
View Trial Details
Completed

INcreased Sun Exposure Without Pain In Research Participants With EPP or XLP

NCT06144840

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Erythropoietic Protoporphyria (EPP), +12 more
Locations
  • Marvel Clinical Research, LLC Huntington Beach, California, United States
  • University of California at San Francisco San Francisco, California, United States
  • University Of Miami School Of Medicine, Center For Liver Diseases Miami, Florida, United States
  • MGH Boston, Massachusetts, United States
View all 35 locations
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